To distinguish the safety and potency of clavipectoral fascial plane block with interscalene brachial plexus block in clavicular surgeries along with superficial cervical plexus block
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/08/056701
- Lead Sponsor
- SAVITHA S
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patient aged between 18 to 60 years of age.
2.Patient of either gender.
3.ASA-PS 1 or ASA-PS II .
4.Patient will be posted for elective internal fixation of clavicle fracture
Exclusion Criteria
1.Patient who refuse to participate.
2.Patient belonging to ASA-PS III and above.
3.Patient with respiratory insufficiency (bilateral rib fractures, obstructive emphysema).
4.Patient with abnormal blood coagulation.
5.Patient with puncture site infection.
6.Patients who cannot lie down / non-co-operative / psychiatric illness.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Determine the probability of hemi-diaphragmatic paresis in both groups measured by calculating hemi-diaphragmatic excursion during sigh test.Timepoint: The range of diaphragmatic movement from the expiratory position to deep inspiration (sigh test) was recorded before & 30 min after the block.
- Secondary Outcome Measures
Name Time Method To compare onset of sensory block by using cold swab test in both groupsTimepoint: 1-10 mins;compare the intraoperative hemodynamic effect in both groups.Timepoint: intraoperative-10 min <br/ ><br>before block & <br/ ><br>5,10,20,30,45,60,75,90,105,120150,180 <br/ ><br>;compare the duration of post op analgesia using visual analogue study (VAS) in both groups.Timepoint: 2,4,6,8 hours